Team:Groningen/Labwork/15 September 2013
From 2013.igem.org
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<br>Colony PCR (NEB Master Mix) was performed on 4 colonies per plate using VF2 and VR primers (annealing temperature 65°C). | <br>Colony PCR (NEB Master Mix) was performed on 4 colonies per plate using VF2 and VR primers (annealing temperature 65°C). | ||
<br>The samples were checked on agarose gel 0.8%. | <br>The samples were checked on agarose gel 0.8%. | ||
- | <br> | + | <br>The gel didn't run well, however, one colony per plate was inoculated in LB + Cm for further screening. |
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Revision as of 14:18, 15 September 2013
Claudio
Plates containing pSB1C3-S1-S5-S5-S13 and pSB1C3-S2-S5-S5-S14 showed thousands of colonies.Colony PCR (NEB Master Mix) was performed on 4 colonies per plate using VF2 and VR primers (annealing temperature 65°C).
The samples were checked on agarose gel 0.8%.
Colony C from pSB1C3-S1-S5-S5-S13 and colony A from pSB1C3-S2-S5-S5-S14 showed to be positive candidates and were inoculated in LB + Cm.
Plates containing pSB1C3-S16-S3-S5-S13 and pSB1C3-S16-S9-S11-S14 showed thousands of colonies.
Colony PCR (NEB Master Mix) was performed on 4 colonies per plate using VF2 and VR primers (annealing temperature 65°C).
The samples were checked on agarose gel 0.8%.
The gel didn't run well, however, one colony per plate was inoculated in LB + Cm for further screening.